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Results for “K3Pro Temporary abutment”

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Registry EUDAMED 79 FDA 510(k) incl. De Novo FDA PMA GUDID 43

Country / market European Union (all) 79 United States 43

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Germany 79

Risk class Class I Class IIa Class IIb 79 Class III Class II (US)

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Class A Class B Class C Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

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79 devices foundsorted by relevance

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K3Pro Temporary abutment

Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG,Germany Group of variants

Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:IIb
K3Pro Temporary abutment

Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG,Germany Group of variants

Active Regimes: CE MDD Registry: EUDAMED Class:IIb

Showing 41-60 of 79

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